Children's Medical Research Institute, Genome Integrity Group, Westmead, NSW, Australia.
University of Sydney, Sydney Medical School, Sydney, NSW, Australia.
Sci Rep. 2016 Jun 29;6:29030. doi: 10.1038/srep29030.
The enteric disease coccidiosis, caused by the unicellular parasite Eimeria, is a major and reoccurring problem for the poultry industry. While the molecular machinery driving host cell invasion and oocyst wall formation has been well documented in Eimeria, relatively little is known about the host cell modifications which lead to acquisition of nutrients and parasite growth. In order to understand the mechanism(s) by which nutrients are acquired by developing intracellular gametocytes and oocysts, we have performed uptake experiments using polystyrene nanoparticles (NPs) of 40 nm and 100 nm in size, as model NPs typical of organic macromolecules. Cytochalasin D and nocodazole were used to inhibit, respectively, the polymerization of the actin and microtubules. The results indicated that NPs entered the parasite at all stages of macrogametocyte development and early oocyst maturation via an active energy dependent process. Interestingly, the smaller NPs were found throughout the parasite cytoplasm, while the larger NPs were mainly localised to the lumen of large type 1 wall forming body organelles. NP uptake was reduced after microfilament disruption and treatment with nocodazole. These observations suggest that E. maxima parasites utilize at least 2 or more uptake pathways to internalize exogenous material during the sexual stages of development.
由单细胞寄生虫球虫引起的肠道疾病球虫病是家禽业的一个主要且反复出现的问题。虽然 Eimeria 中宿主细胞入侵和卵囊壁形成的分子机制已经得到很好的记录,但对于导致获取营养物质和寄生虫生长的宿主细胞修饰相对知之甚少。为了了解内细胞配子体和卵囊获取营养物质的机制,我们使用 40nm 和 100nm 大小的聚苯乙烯纳米颗粒(NPs)作为典型的有机大分子模型 NPs 进行了摄取实验。细胞松弛素 D 和诺考达唑分别用于抑制肌动蛋白和微管的聚合。结果表明,NPs 通过主动能量依赖的过程进入处于大配子体发育和早期卵囊成熟各个阶段的寄生虫。有趣的是,较小的 NPs 遍布整个寄生虫细胞质,而较大的 NPs 主要定位于大型 1 型壁形成体腔细胞器的腔中。微丝破坏和用诺考达唑处理后,NP 摄取减少。这些观察结果表明,E. maxima 寄生虫在有性发育阶段至少利用 2 种或更多的摄取途径内化外源性物质。